Organic nitroso compounds
Medchemexpress LLC N-Nitroso-N-methylurea | 684-93-5 | 99.7% | 103.08 | 2 G
N-Nitroso-N-methylurea is a potent carcinogen, mutagen, and teratogen. It acts as a direct-acting alkylating agent that interacts with DNA, targeting multiple animal organs to cause various cancers and/or degenerative diseases. It is also a precursor in the synthesis of diazomethane.
- Potent carcinogen, mutagen, and teratogen
- Direct-acting alkylating agent that interacts with DNA
- Targets multiple animal organs to cause various cancers and/or degenerative diseases
- Precursor in the synthesis of diazomethane
- For research use only
Cayman Chemical N-NItroso FluoxetIn 10mg
A derivative of fluoxetine; genotoxic to S. typhimurium at 0.06-0.12 mg/ml
Medchemexpress LLC TANDSOPIRONE 50.0MG
Tandospirone /SM-3997/ is a potent and selective 5-HT1A receptor partial agonist with a Ki of 27 nM. Tandospirone has anxiolytic and antidepressant activities. Tandospirone can be used for the research of the central nervous system disorders and the underlying mechanisms.For research use only.
World Precision Instrument SNAP S-Nitroso-N-acetyl-D-penicillamine-SNAP50
SNAP is a stable green crystalline S-nitrosothiol compound that mimics the action of nitric oxide in vivo. It has vasodilatory properties and has been shown to relax isolated bovine coronary artery rings by activating soluble granulate cyclase. This reagent also actuates apoptosis in mouse thymocytes and has been accounted for reversible inactivation of protein Kinase C. SNAP can be used for calibration of all WPI NO sensors. Call for details. M.W. 220.2, Purity > 98% by NMR or TLC.
Cayman Chemical N-NItroso-N-ethylnIlIn 25mg
An N-nitrosamine; non-carcinogenic in a survival assay using 2FR450 Rauscher leukemia virus-infected rat embryo cultures; a synthetic intermediate in the synthesis of 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones as CXCR2 antagonists
Cayman Chemical N-NItroso-N-methylnIlIn 100mg
An N-nitrosamine; induces the formation of esophageal, pharyngeal, and tongue tumors in rats at 200 mg/L in the drinking water or 15 mg/ml via oral gavage; toxic to rats (LD50s = 336 and 225 mg/kg for male and female rats, respectively); reduces survival of hamsters but only induces a low incidence of tumors at 5 mg/week for a total dose of 1.8 mmol
Medchemexpress LLC BUSPIRONE 50.0MG
Buspirone is an orally active 5-HT1A receptor agonist, and a dopamine D2 autoreceptorsant antagonist. Buspirone is an anxiolytic agent and can be used for the generalized anxiety disorder research.
Sigma Aldrich Fine Chemicals Biosciences Isopentyl nitrite 96% | 110-46-3 | MFCD00002057 | 100ML
Isopentyl nitrite 96% | Purity: 96% | Mol Wt: 117.15 | 110-46-3 | MFCD00002057 | 100ML
Medchemexpress LLC N-Nitrosomorpholine | 59-89-2 | 99.9% | 1 G
N-Nitrosomorpholine is a photosensitive nitrosamine known for its carcinogenic properties, primarily used in research to construct animal cancer models. It is intended for research applications only and not for patient use.
- Carcinogenic agent for research purposes.
- Used to construct animal cancer models.
- Induces liver disease, including cytoplasmic and nuclear changes.
- Causes toxic damage, single-cell necrosis, and loss of glycogen.
- Promotes giant cell production, bile duct proliferation, and fibrosis.
- Leads to cirrhosis and metastatic liver cancer in animal models.
- Supports the study of molecular and histological changes, including increased serum glutamate-oxaloacetate aminotransferase levels and liver damage.
Medchemexpress LLC N-Nitrosomorpholine | 59-89-2 | 99.98% | 5 G
N-Nitrosomorpholine is a photosensitive nitrosamine that is carcinogenic and can be used to construct animal cancer models. It is for research use only and not sold to patients.
- Photosensitive nitrosamine
- Carcinogenic agent
- Used to construct animal cancer models
- For research use only
- Not sold to patients
Medchemexpress LLC Tripeptide epoxyketone immunoproteasome (LMP-7) inhibitor | 1416709-79-9 | 98.9% | 618.72 g/mol | C37H38N4O5 | 50MG
A selective tripeptide epoxyketone inhibitor of the immunoproteasome LMP7 subunit for biochemical and cellular research. It covalently modifies proteasomal N-terminal threonine active sites and has demonstrated antitumor activity in preclinical studies.
- Selective LMP7 (β5i) immunoproteasome inhibitor.
- Covalently modifies N-terminal threonine active sites.
- Reported IC50 of 22 nM against LMP7.
- Demonstrated inhibition of multiple myeloma cell growth and induction of apoptosis.
- High chemical purity (98.9%).
- Enantiomeric excess 100%.
- Molecular weight 618.72 g/mol and formula C37H38N4O5.
- Supplied in small research pack sizes, e.g., 50 mg.
- For research use only; not for human use.
Enzo Life Sciences Spermine NONOate (25mg). CAS: 136587-13-8
Nitric oxide (NO) donor. A convenient reagent for preparing aqueous solutions of NO. Alternative name: SPER/NO, (Z)-1-N-[3-Aminopropyl]-N-[4-(3-aminopropylammonio)butyl]-amino-diazen-1-ium-1,2-diolate. Purity: ≥97% (NMR). Appearance: White to off-white crystalline solid. Solubility: Soluble in water, methanol or 100% ethanol. Long Term Storage: -80°C.
Spermine NONOate 97%, Thermo Scientific™
CAS: 136587-13-8 Molecular Formula: C10H26N6O2 Molecular Weight (g/mol): 262.358 InChI Key: QPIOUFBAROSIAN-UHFFFAOYSA-N Synonym: spermine nonoate,spermine-nitric oxide,spermine nitric oxide complex,noc 22,noc-22,spermine nitric oxide adduct,spermine/nitric oxide complex,ccris 4091,sper/no,sper-no PubChem CID: 5259 IUPAC Name: N-[3-aminopropyl-[4-(3-aminopropylamino)butyl]amino]-N-hydroxynitrous amide SMILES: C(CCN(CCCN)N(N=O)O)CNCCCN